Increasing preservation efficiency and product quality through control of temperature distributions in high pressure applications

The effectiveness of HP sterilisation is a function of both temperature and pressure. As during pressurisation the product temperature increases, heat transfer to the colder HPP vessel wall occurs and the product fraction near the vessel wall will be colder than the product in the middle of the vessel. The effect of the temperature distribution in the vessel on the inactivation of Bacillus stearothermophilus has been examined. A mathematical model has been built, in which both thermodynamics and inactivation kinetics are integrated. Heat transfer is based on a Finite Element simulation, inactivation kinetics are based on first order kinetics. Based on this model and experiments the effect of an homogeneous temperature distribution on inactivation is demonstrate

Increasing preservation efficiency and product quality through control of temperature distributions in high pressure applications

The effectiveness of HP sterilisation is a function of both temperature and pressure. As during pressurisation the product temperature increases, heat transfer to the colder HPP vessel wall occurs and the product fraction near the vessel wall will be colder than the product in the middle of the vessel. The effect of the temperature distribution in the vessel on the inactivation of Bacillus stearothermophilus has been examined. A mathematical model has been built, in which both thermodynamics and inactivation kinetics are integrated. Heat transfer is based on a Finite Element simulation, inactivation kinetics are based on first order kinetics. Based on this model and experiments the effect of an homogeneous temperature distribution on inactivation is demonstrate

Assay of Kanamycin A by HPLC with Direct UV Detection

The development of a simple reversed phase ion pair liquid chromatographic method for the assay of kanamycin A has been described. Because of the lack of a UV chromophore in the structure of kanamycin A, borate complexation was used to allow direct UV detection at 205 nm. Three columns were evaluated in this study: Zorbax Extend C18 (4.6 mm × 250 mm; 5 μm), XBridge C18 (4.6 mm × 250 mm; 5 μm) and apHera C18 (4.6 mm × 250 mm; 5 μm). The mobile phase was a mixture of 0.1 M disodium tetraborate (pH 9.0) and water (20:80, v/v) supplemented with 0.5 g L-1 sodium octanesulphonate. Final chromatographic conditions were achieved on the XBridge column at 50 C. The method was validated according to ICH guidelines and applied to a commercially available sample. It is much faster and more specific than the current microbiological assay prescribed in the European Pharmacopoeia. No expensive equipment is necessary to perform this assay making it a viable replacement. © 2013 Springer-Verlag Berlin Heidelberg.status: publishe